Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Hereditary Motor and Sensory-Neuropathy Type II
6 138 3 0.27 2 1.3E-02
DIABETES MELLITUS, PERMANENT NEONATAL
6 0 3 0.27 0 0
CUI: C0342283
Disease: Hyperproinsulinemia
Hyperproinsulinemia
2 0 2 0.25 0 0
Congenital Generalized Lipodystrophy Type 2
2 0 2 0.25 0 0
DIABETES MELLITUS, INSULIN-DEPENDENT, 2
2 0 2 0.25 0 0
CUI: C2931276
Disease: Spastic paraplegia 17
Spastic paraplegia 17
2 0 2 0.25 0 0
Maturity-onset diabetes of the young, type 10
2 0 2 0.25 0 0
ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY
2 0 2 0.25 0 0
CUI: C0221032
Disease: Familial generalized lipodystrophy
Familial generalized lipodystrophy
8 0 3 0.23 0 0
Familial Partial Lipodystrophy, Type 3
3 0 2 0.22 0 0
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus
4 0 2 0.20 0 0
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V
4 0 2 0.20 0 0
Insulin-resistant diabetes mellitus at puberty
5 0 2 0.18 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
6 0 2 0.17 0 0
Latent Autoimmune Diabetes in Adults
6 0 2 0.17 0 0
CUI: C1969875
Disease: Beta-cell dysfunction
Beta-cell dysfunction
6 0 2 0.17 0 0
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
36 30 6 0.16 14 0.45
Maturity onset diabetes mellitus in young
14 0 3 0.16 0 0
CUI: C4073162
Disease: Elevated hemoglobin A1c
Elevated hemoglobin A1c
14 0 3 0.16 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 3 0.16 0 0
CUI: C1856904
Disease: Reduced pancreatic beta cells
Reduced pancreatic beta cells
7 0 2 0.15 0 0
CUI: C1847425
Disease: Abnormal oral glucose tolerance
Abnormal oral glucose tolerance
15 0 3 0.15 0 0
CUI: C0206669
Disease: Hepatocellular Adenoma
Hepatocellular Adenoma
16 0 3 0.14 0 0
CUI: C1837802
Disease: Decreased serum leptin
Decreased serum leptin
8 0 2 0.14 0 0
CUI: C2748055
Disease: Hypoinsulinaemia (disorder)
Hypoinsulinaemia (disorder)
16 0 3 0.14 0 0